Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
  • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
  • C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D241/00—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings
  • C07D241/36—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems
  • C07D241/38—Heterocyclic compounds containing 1,4-diazine or hydrogenated 1,4-diazine rings condensed with carbocyclic rings or ring systems with only hydrogen or carbon atoms directly attached to the ring nitrogen atoms
  • C07D241/40—Benzopyrazines
  • C07D241/44—Benzopyrazines with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to carbon atoms of the hetero ring
• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
  • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
  • C07D471/04—Ortho-condensed systems

Definitions

• This invention relates to novel sulfoxide derivatives and processes for the preparation of the same.
• N-cyano-N'- methyl- N"-[2-[[(5-methyl-1H-imidazol-4-yl)methyl]thio]-ethyl]guanidine (available as tradename of Cimetidine) is well known.
• H + +K + ATPase plays a principal roll in the final secretion mechanism of gastric acid in stomach cells [Scand. J. Gastroenterol., 14, 131-135 (1979)].
• As a substance having H + +K + ATPase inhibitory activity Norinium bromide is known [Proceeding of the Society for Experimental Biology and Medicine, 172, 308-315(1983)].
• an object of the present invention is to provide novel sulfoxide derivatives which is of value as an anti-ulcer agent.
• a sulfoxide derivative having the formula (I): wherein each of R 1 and R 2 independently is hydrogen or an alkyl group having 1 to 6 carbon atoms, and each of R 3 , R 4 , R 4a and R 4b independently is hydrogen, halogen, an alkoxy group having 1 to 6 carbon atoms which may be substituted with fluorine atom(s), or an alkyl group ; having 1 to 6 carbon atoms, or trifluoromethyl.
• a sulfoxide derivative having the formula (V): wherein each of R 5 and R 6 independently is hydrogen, halgoen, an alkyl group having 1 to 6 carbon atoms, or an alkoxy group having 1 to 6 carbon atoms, R 7 is hydrogen, an alkyl group having 1 to 6 carbon atoms, or an alkoxy group having 1 to 6 carbon atoms, Y is CH or N, and Z is unsubstituted or substituted 2-pyridyl or a 2-aminophenyl group having the formula (VI): wherein each of R 8 and R 9 independently is hydrogen or an alkyl group having 1 to 6 carbon atoms, and the phenyl group may be substituted.
• substituents attachable to the 2-pyridyl group and the phenyl group include halogen, an alkyl group (preferably having 1 to 6 carbon atoms), and an alkoxy group (preferably having 1 to 6 carbon atoms).
• each of R 3 , R 4 , R 4a and R 4b is hydrogen
• R 1 and R 2 preferably is an alkyl group having 1 to 6 carbon atoms such as methyl or ethyl.
• Representative examples of the compounds of the formula (I) include:
• the sulfoxide derivative having the formula (I) can be advantageously prepared by a process which comprises:
• the starting compound having the formula (II) can be prepared by bringing a diaminopyridine or its derivative into contact potassium xanthogenate in an alcoholic solvent.
• the reactive group (X) of the compound having the formula (III) can be a halogen atom such as chlorine or bromine; a sulfonyloxy group such as methylsulfonyl or tolunesulfonyl; or acetoxy.
• the reaction of the compound (II) and the compound (III) can be performed at a temperature from room temperature to the reflux temperature for 30 min. to 24 hrs., in an inert solvent such as benzene, ethanol or acetone.
• the reaction can be carried out in the presence of an alkali agent such as NaOH, KOH, K 2 CO 3 or NaHCO 3 , for trapping an acid produced in the reaction.
• the salt of the compound (III) can be an inorganic acid salt such as hydrochloride or sulfate, or an organic acid salt such as benzoate.
• the oxidation of the compound (IV) can be performed in the conventional manner.
• the compound (IV) can be oxidized using an oxidizing agent such as hydrogen peroxide, an organic peroxide (e.g., m-chloroperbenzoic acid), or sodium hydrochlorite.
• the reaction can be performed in an inert solvent such as chloroform, dichloromethane, methanol, or ethyl acetate at a temperature ranging from -30°C to 50°C, preferably -15°C to 5°C.
• each of R 5 , R 6 and R 7 is hydrogen
• R and R 9 preferably is an alkyl group having 1 to 6 carbon atoms such as methyl or ethyl.
• Representative examples of the compounds of the formula (V) include:
• the sulfoxide derivative having the formula (V) can be advantageously prepared by a process which comprises:
• the starting compound having the formula (VII) can be prepared from a diamino compound in the conventional nanner.
• 2-mercapto-3-methylquinoxaline can be prepared by a process described in J. Org. Chem., 21, 470 (1956).
• the reactive group (Q) of the compound having the formula (VIII) can be a halogen atom such as chlorine or bromine; a sulfonyloxy group such as methylsulfonyl or tolunesulfonyl; or acetoxy.
• the reaction of the compound (VII) and the compound (VIII) can be performed at a temperature from room temperature to the reflux temperature for 30 min. to 24 hrs., in an inert solvent such as benzene, ethanol or acetone.
• the reaction can be carried out in the presence of an alkali agent such as NaOH, KOH, K 2 C0 3 or NaHC0 3 , for trapping an acid produced in the reaction.
• the salt of the compound (VIII) can be an inorganic acid salt such as hydrochloride or sulfate, or an organic acid salt such as benzoate.
• the oxidation of the compound (IX) can be performed in the conventional manner.
• the compound (IX) can be oxidized using an oxidizing agent such as hydrogen peroxide, an organic peroxide (e.g., m-chloroperbenzoic acid), or sodium hypochlorite.
• the reaction can be performed in an inert solvent such as chloroform, dichloromethane, methanol, or ethyl acetate at a temperature ranging from -30°C to 50°C, preferably -15°C to 5°C.
• the sulfoxide derivatives of the formula (I) or (V) according to the invention are of value as a cytoprotective agent for gastrointestinal tract and can be utilized for the treatment or prevention of a non-gastric-acid-induced, non- traumatically-induced, non-neoplastic gastrointestinal inflammatory disease in a mammal suffering from or particularly susceptible to the development of said disease, as disclosed in U.S. Patent No. 4,359,465 (Ruwart).
• the anti-ulcer agent for gastrointestinal tract containing a sulfoxide derivative of the formula (I) or (V) can be administered orally or parenterally.
• preparation forms for oral administration include tablets, capsules powder, granules, and syrup.
• excipients there can be used excipients, disintegrants, binders, lubricants, pigments, diluents and the like which are commonly employed in the art.
• excipients include dextrose and lactose.
• examples of the disintegrants include starch and carboxymethylcellulose.
• the lubricants include magnesium stearate and talc.
• binders include hydroxypropylcellulose, gelatin and polyvinylpyrrolidone.
• the dose is generally not more than 500 mg/day, preferably about 100 ug/day to 300 mg/day, for an adult.
• the dose can be either increased or decreased depending upon the age and other conditions.
• gastric acid secretory cells of a rabbit gastric mucosa were isolated and vesicle containing H + +K + ATPase was prepared by centrifuging the cells in Ficoll of discontinuous density gradient. After the enzyme was incubated at room temperature for 25 min. in 0.5 mi of a solution which contained 5 mM of an imidazole buffer (pH 6.0) and 2 x 10 -4 M of each test compound, the mixture was heated to 37°C at which it was allowed to stand for further 5 min.
• an imidazole buffer pH 6.0
• Cimetidine (tradename of N-cyano-N'-methyl-N"-[2-[[(5-methyl-1H-imidazol-4-yl)methyl]thio]ethyl]-guanidine)
• Rats fasted for 24 hours before experiments were placed in a restraint cage.
• the animals were immersed vertically to the level of the xiphoid process in a water bath (21°C) for 7 hours and then killed.
• the stomach of each rat was removed and inflated by injecting 10 ml of 1% formalin to fix the inner and outer layers of the gastric walls. This formalin treatment was performed in all of the following experiments. Subsequently, the stomach was incised along a greater curvature and examined for any erosion in the glandular portion. Each test compound or a vehicle alone was given orally 10 minutes before stressing.
• a hydrochloric acid-ethanol solution (150 mM HCl in 60% ethanol) was given orally to rats in a dose of 1 ml/200g, which rats had been fasted for 24 hours before experiments. One hour later, each animal was killed and the stomach was examined for any erosion in the glandular portion. Each test compound or a vehicle alone was given orally 30 minutes before ethanol treatment.
• the organic layer was washed successively with 5% aqueous sodium hydroxide solutin, water and saturated aqueous sodium chloride solution, and then dried over sodium sulfate.
• the sodium sulfate was removed by filtration, and the solvent was removed to give a residue.
• the residue was warmed in ether, and the insolubles were removed by fitration.
• IR cm -1 1590, 1470, 1430, 1360, 1200, 1200, 1080, 1050, 995, 960, 765, 745
• IR -1 1590, 1160, 1090, 1080, 1070, 1045, 945, max 760
• IR -1 2930, 1490, 1480, 1445, 1090, 1070, max 1050 , 870, 760

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Nitrogen Condensed Heterocyclic Rings (AREA)
• Pyridine Compounds (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

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• 1987
  • 1987-01-10 KR KR1019870000149A patent/KR950001015B1/ko not_active IP Right Cessation
  • 1987-01-12 DE DE8787300228T patent/DE3770020D1/de not_active Expired - Fee Related
  • 1987-01-12 EP EP87300228A patent/EP0234690B1/de not_active Expired - Lifetime
  • 1987-01-12 CA CA000527149A patent/CA1304087C/en not_active Expired - Fee Related
  • 1987-01-12 AU AU67492/87A patent/AU604668B2/en not_active Ceased
  • 1987-01-12 ES ES198787300228T patent/ES2032436T3/es not_active Expired - Lifetime
  • 1987-01-22 AR AR87306447A patent/AR246263A1/es active
• 1988
  • 1988-05-24 US US07/198,086 patent/US4933458A/en not_active Expired - Fee Related
• 1990
  • 1990-04-09 US US07/506,171 patent/US5106976A/en not_active Expired - Fee Related

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